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Mechanisms of Photoaging and Cutaneous Photocarcinogenesis, and Photoprotective Strategies with Phytochemicals

机译:光老化和皮肤光致癌的机理以及植物化学物质的光保护策略

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Photoaging and photocarcinogenesis are primarily due to solar ultraviolet (UV) radiation, which alters DNA, cellular antioxidant balance, signal transduction pathways, immunology, and the extracellular matrix (ECM). The DNA alterations include UV radiation induced thymine-thymine dimers and loss of tumor suppressor gene p53. UV radiation reduces cellular antioxidant status by generating reactive oxygen species (ROS), and the resultant oxidative stress alters signal transduction pathways such as the mitogen-activated protein kinase (MAPK), the nuclear factor-kappa beta (NF-κB)/p65, the janus kinase (JAK), signal transduction and activation of transcription (STAT) and the nuclear factor erythroid 2-related factor 2 (Nrf2). UV radiation induces pro-inflammatory genes and causes immunosuppression by depleting the number and activity of the epidermal Langerhans cells. Further, UV radiation remodels the ECM by increasing matrixmetalloproteinases (MMP) and reducing structural collagen and elastin. The photoprotective strategies to prevent/treat photoaging and photocarcinogenesis include oral or topical agents that act as sunscreens or counteract the effects of UV radiation on DNA, cellular antioxidant balance, signal transduction pathways, immunology and the ECM. Many of these agents are phytochemical derivatives and include polyphenols and non-polyphenols. The flavonoids are polyphenols and include catechins, isoflavones, proanthocyanidins, and anthocyanins, whereas the non-flavonoids comprise mono phenolic acids and stilbenes. The natural sources of polyphenols include tea, cocoa, grape/wine, soy, pomegranate, and Polypodium leucotomos. The non-phenolic phytochemicals include carotenoids, caffeine and sulphoraphance (SFN). In addition, there are other phytochemical derivatives or whole extracts such as baicalin, flavangenol, raspberry extract, and Photomorphe umbellata with photoprotective activity against UVB radiation, and thereby carcinogenesis.
机译:光老化和光致癌作用主要归因于太阳紫外线(UV)辐射,这会改变DNA,细胞抗氧化剂平衡,信号转导途径,免疫学和细胞外基质(ECM)。 DNA的改变包括紫外线辐射诱导的胸腺嘧啶-胸腺嘧啶二聚体和肿瘤抑制基因p53的丢失。紫外线辐射会通过产生活性氧(ROS)来降低细胞的抗氧化剂状态,产生的氧化应激会改变信号转导途径,例如促分裂原活化蛋白激酶(MAPK),核因子-κβ(NF-κB)/ p65, janus激酶(JAK),信号转导和转录激活(STAT)以及核因子红系2相关因子2(Nrf2)。紫外线辐射通过减少表皮朗格汉斯细胞的数量和活性来诱导促炎基因并引起免疫抑制。此外,紫外线辐射通过增加基质金属蛋白酶(MMP)和减少结构性胶原蛋白和弹性蛋白来重塑ECM。预防/治疗光老化和光致癌作用的光保护策略包括充当防晒剂或抵消UV辐射对DNA,细胞抗氧化剂平衡,信号转导途径,免疫学和ECM的作用的口服或局部用药。这些试剂中的许多是植物化学衍生物,包括多酚和非多酚。类黄酮是多酚,包括儿茶素,异黄酮,原花青素和花色苷,而非类黄酮则包含单酚酸和丁苯二酚。多酚的天然来源包括茶,可可,葡萄/葡萄酒,大豆,石榴和白粉病。非酚类植物化学物质包括类胡萝卜素,咖啡因和硫丹(SFN)。此外,还有其他植物化学衍生物或完整提取物,例如黄ical苷,黄烷醇,覆盆子提取物和伞形变种,对UVB辐射具有光保护活性,从而具有致癌作用。

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